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83-41-0

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83-41-0 Usage

Chemical Properties

CLEAR YELLOWISH LIQUID AFTER MELTING

Uses

Different sources of media describe the Uses of 83-41-0 differently. You can refer to the following data:
1. 3-Nitro-o-xylene is a useful benzene-derived building block, and has aquatic toxicity properties.
2. 1,2-Dimethyl-3-nitrobenzene (3-Nitro-o-xylene) was used to prepare 2-methyl-3-nitrobenzylidene diacetate. It was also used to dissolve sodium-selective ligand.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

3-Nitro-o-xylene is incompatible with strong oxidizers and strong bases .

Fire Hazard

3-Nitro-o-xylene is combustible.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 83-41-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83-41:
(4*8)+(3*3)+(2*4)+(1*1)=50
50 % 10 = 0
So 83-41-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO2/c1-6-4-3-5-8(7(6)2)9(10)11/h3-5H,1-2H3

83-41-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B24917)  3-Nitro-o-xylene, 99%   

  • 83-41-0

  • 100g

  • 182.0CNY

  • Detail
  • Alfa Aesar

  • (B24917)  3-Nitro-o-xylene, 99%   

  • 83-41-0

  • 500g

  • 901.0CNY

  • Detail
  • Sigma-Aldrich

  • (40870)  1,2-Dimethyl-3-nitrobenzene  Selectophore, ≥99.0%

  • 83-41-0

  • 40870-25ML

  • 3,185.91CNY

  • Detail
  • Aldrich

  • (130303)  1,2-Dimethyl-3-nitrobenzene  97%

  • 83-41-0

  • 130303-100G

  • 391.95CNY

  • Detail

83-41-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Nitro-o-xylene

1.2 Other means of identification

Product number -
Other names Benzene, 1,2-dimethyl-3-nitro-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:83-41-0 SDS

83-41-0Relevant articles and documents

Self-powered continuous nitration method and device

-

Paragraph 0057-0060, (2021/07/17)

The invention belongs to the technical field of organic synthesis application, and particularly relates to a self-powered continuous nitration method and device. According to the method, a raw material (or a raw material solution) and mixed acid (or nitric acid) are added into a self-powered continuous reactor at the same time, reaction feed liquid continuously and circularly flows, is mixed and reacts in a tube pass through self-propelling force generated by stirring of an impeller, the mass and heat transfer process is completed, and the target requirement is met. According to the invention, the mass transfer and heat transfer efficiency can be improved, the heat exchange and heat transfer capabilities are improved, the reaction time is shortened, the risk degree of art is reduced, the thermal runaway risk is avoided, the reaction safety is improved, and the realization of chemical industry intrinsic safety large scale production is facilitated.

2-methyl-3-methoxybenzoyl chloride synthesizing process

-

Paragraph 0014; 0019; 0024, (2019/03/15)

The invention discloses a 2-methyl-3-methoxybenzoyl chloride synthesizing process. According to the present invention, low-cost o-xylene is used as a starting raw material, the product is synthesizedby using a conventional synthesis method comprising nitrification, esterification, reduction, diazotization, methylation, acyl chlorination and other steps, and the total yield is controlled at more than 65%; the esterification of the intermediate product improves the separation degree of the intermediate; the reaction solvent is added in the diazotization step, such that the process parameters are relatively easy to control, and the purity of the intermediate in the diazotization step is more than 96% so as to provide the guarantee for the quality of the subsequent product; and with the synthesis process, the product quality is stable and reliable, and the cost is low.

Hydrophobic WO3/SiO2 catalyst for the nitration of aromatics in liquid phase

Kulal,Kasabe,Jadhav,Dongare,Umbarkar

, p. 105 - 113 (2019/02/15)

WO3/SiO2 solid acid catalyst synthesized using sol gel method has shown promising activity (up to 65% conversion) for aromatic nitration in liquid phase using commercial nitric acid (70%) as nitrating agent without using any sulfuric acid. The water formed during the reaction as well as water from dilute nitric acid (70%) was removed azeotropically, however due to the hydrophilic nature of the catalyst, some water gets strongly adsorbed on catalyst surface forming a barrier layer between catalyst and organics. This prevents effective adsorption of substrate on catalyst surface for its subsequent reaction. To improve the activity further, the hydrophilic/hydrophobic nature of the catalyst was altered by post modification by grafting with commercial short chain organosilane (Dynasylan 9896). The modified 20% WO3/SiO2 catalyst when used for o-xylene nitration in liquid phase, showed significant increase in the conversion from 65% to 80% under identical reaction conditions. Catalyst characterization revealed decrease in the surface area of 20% WO3/SiO2 from 356 m2/g to 302 m2/g after grafting with Dynasylan 9896. The fine dispersion of WO3 particles (2–5 nm) on silica support was not affected due to modification. NMR and FTIR study revealed the decrease in surface hydroxyl groups imparting hydrophobicity to the catalyst. Interestingly the total acidic sites of the catalyst remained almost unaltered (0.54 mmol NH3/g) even after modification. Even though, the acidity and other characteristics of the catalyst did not change appreciably, there was a considerable increase in the o-xylene conversion which can be ascribed to the hydrophobic nature of the catalyst.

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